3636-03-1

Basic information

• Product Name: Cyclohexanone, 3-(3-butenyl)-
• Synonyms: 3-(Buten-(3)-yl)-cyclohexanon;3-(3-butenyl)cyclohexan-1-one;3-(3'-butenyl)cyclohexanone;Cyclohexanone,3-(3-butenyl);3-(But-3-enyl)-cyclohexanone;1--cyclohexanon-(3);
• CAS NO: 3636-03-1
• Molecular Formula: C10H16O
• Molecular Weight: 152.236
• Mol File: 3636-03-1.mol

Chemical Properties

• CAS DataBase Reference: Cyclohexanone, 3-(3-butenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclohexanone, 3-(3-butenyl)-(3636-03-1)
• EPA Substance Registry System: Cyclohexanone, 3-(3-butenyl)-(3636-03-1)

Safety Data

• Hazardous Substances Data: 3636-03-1(Hazardous Substances Data)

Upstream product

• 145102-57-4 ((3-(but-3-en-1-yl)cyclohex-1-en-1-yl)oxy)trimethylsilane 
• 109323-25-3 1-methyl-3-(3-butenyl)cyclohexyl hydroperoxide 
• 109323-26-4 3-But-3-enyl-1-ethyl-cyclohexyl-hydroperoxide 
• 109323-27-5 3-But-3-enyl-1-phenyl-cyclohexyl-hydroperoxide 
• 22627-45-8 3-(3-butenyl)cyclohex-2-en-1-one 
• 930-68-7 cyclohexenone 
• 109323-34-4 3-But-3-enyl-1-methyl-cyclohexanol 
• 5323-87-5 3-Ethoxycyclohex-2-en-1-one 

Downstream Products

• 130660-18-3 3-(4-Iodobutyl)cyclohexan-1-one 
• 172687-22-8 2-(3-Oxo-cyclohexylmethyl)-acrylic acid methyl ester 
• 172687-17-1 2-(3-Oxo-cyclohexylmethyl)-acrylic acid 
• 159531-88-1 2-(3-Oxo-cyclohexylmethyl)-propenal 
• 113335-14-1 3-(3-Oxo-butyl)-cyclohexanone 
• 135052-04-9 3-(2-[1,2,4]Trioxolan-3-yl-ethyl)-cyclohexanone 
• 90976-56-0 1-(4-Brom-butyl)-cyclohexanon-⁽³⁾ 
• 1111166-00-7 acetic acid 3-but-3-enyl-1-ethynyl-cyclohexyl ester 

Relevant articles and documents

Simple construction of bicyclo[4.3.0]nonane, bicyclo[3.3.0]octane, and related benzo derivatives by palladium-catalyzed cycloalkenylation

(equation presented) Bicyclo[4.3.0]nonanes (hydrindanes) and bicyclo[3.3.0]octanes (octahydropentalenes) are easily synthesized by palladium-catalyzed cycloalkenylations. Additionally, benzo-fused bicyclo[3.3.0]octanes are prepared for the first time thro

A Facile Synthesis of Bicycloalkan-1-ols. Evidence for Organosamarium Intermediates in the Samarium(II) Iodide Promoted Intramolecular Barbier-Type Reaction

Samarium(II) iodide (SmI2) has been successfully employed as a reductive coupling agent for the intramolecular Barbier-type synthesis of bicycloalkan-1-ols.Thus, a variety of 3-(ω-iodoalkyl)cycloalkanones, upon treatment with SmI2 and a catalytic q

FREE RADICAL CARBOCYCLIC RING RECONSTRUCTION

Alkenyl radical generated by β-fragmentation of tertiary cyclohexyloxy radical with carbocyclic ring opening, possessing a suitably located olefinic double bond, undergoes to the intramolecular 5-exo-trigonal cyclization and a new carbocyclic ring was for